The Recall Desk

State

Massachusetts product recalls

72,919 recalls have nationwide distribution and so reach Massachusetts. 8,208 additional recalls listed Massachusetts specifically in their distribution scope.

What the numbers show

Total
8,208
Critical
1,171
Severe
2,012
Most recent
2026-09-09

Of the 8,208 recalls naming Massachusetts we have scored against our rubric, 1,171 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,012 (25%) are Severe.

These figures cover only the 8,208 recalls whose distribution notice names Massachusetts specifically. The 72,919 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2301–2325 of 81127

  • HighCPSC·26429·2026-04-23

    mGanna Sodium Hydroxide Pellet Bags Recalled Over Chemical Burn Risk

    mGanna sodium hydroxide pellet bags sold on Amazon by Archie Xpress are recalled because the packaging is not child-resistant, risking chemical burns to skin and eyes.

    Product
    mGanna Sodium Hydroxide (lye) Pellet Bags
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V260000·2026-04-23

    2025-2027 Volvo VNL and VNR trucks recalled for brake system defect

    Volvo Trucks is recalling certain 2025-2027 VNL and 2026-2027 VNR vehicles because unprotected electrical connectors on the rear brake modulators can short circuit, disabling anti-lock brakes and stability control.

    Product
    VOLVO — VOLVO VNL (4), VNR (4)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26440·2026-04-23

    KMUYSL barn playset fence handles can detach, posing a choking hazard

    KMUYSL Big Red Barn Farm Animal Playsets are recalled because the fence handles can detach from a toy intended for children under three, violating the small parts ban.

    Product
    KMUYSL Big Red Barn Farm Animal Playsets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26E025000·2026-04-23

    GM Recalls ACDelco Brake Fluid Due to Sediment Contamination

    General Motors is recalling specific lots of ACDelco GMW DOT 3 brake fluid that may contain visible sediment, potentially reducing brake performance.

    Product
    ENGINE AND ENGINE COOLING:ENGINE:OIL/LUBRICATION recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26430·2026-04-23

    Wiifo children's tower stools can collapse or tip over during use

    Wiifo children's tower stools are recalled because they can collapse or tip over and a child's torso can fit through the side openings. 22 incidents and six injuries reported.

    Product
    Wiifo Children's Tower Stools
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V262000·2026-04-23

    Jeep Wagoneer S and Dodge Charger instrument panel displays may fail

    Chrysler is recalling certain Jeep Wagoneer S and Dodge Charger electric vehicles because a software error may cause the instrument panel display to fail, breaching five federal standards.

    Product
    DODGE — DODGE, JEEP CHARGER EV, WAGONEER S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26438·2026-04-23

    Cpzzkq baby lounger padding can obstruct an infant's breathing

    Cpzzkq baby loungers are recalled because they violate the mandatory safety standard for infant support cushions and the padding can obstruct an infant's breathing.

    Product
    Cpzzkq Baby Loungers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26437·2026-04-23

    Sweetie Baby loungers fail the mandatory infant sleep product standard

    Sweetie Baby and Style Life Eleven baby loungers are recalled because their sides are below the minimum height and they have no stand, posing a fall hazard to infants.

    Product
    Sweetie Baby and Style Life Eleven Baby Loungers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26432·2026-04-23

    TOETOL children's tower stools can collapse during use

    TOETOL HOME children's tower stools are recalled because they can collapse or tip over and a child's torso can fit through the side openings. 18 collapses and 11 injuries reported.

    Product
    TOETOL Tower Stools
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V263000·2026-04-23

    2026 Land Rover Defender fuel tank improperly manufactured too thin

    Jaguar Land Rover North America is recalling certain 2026 Land Rover Defender vehicles because the fuel tank was improperly manufactured with walls that are too thin, which may leak fuel in a crash and increase fire risk.

    Product
    LAND ROVER — LAND ROVER DEFENDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1799-2026·2026-04-22

    B. Braun Hemodialysis Bloodlines Recalled Due to Potential Air Bubble Accumulation

    B. Braun Medical Inc is recalling STREAMLINE BLOODLINE SET FOR DIALOG (Model Number: SL-2010M2096) because air bubbles may accumulate in the arterial line.

    Product
    B. Braun Hemodialysis Bloodlines, STREAMLINE BLOODLINE SET FOR DIALOG. Model Number: SL-2010M2096
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V258000·2026-04-22

    Volkswagen Taos fuel pressure sensor may separate in a rear-end crash

    Volkswagen is recalling certain 2025-2026 Taos vehicles because the fuel pressure sensor may dislodge from the fuel tank in a rear-end crash, failing FMVSS 301 fuel system integrity.

    Product
    VOLKSWAGEN — VOLKSWAGEN TAOS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1797-2026·2026-04-22

    Omnipod 5 insulin pods from 49 lots have torn internal cannulas

    Omnipod 5 Pods from 49 lots have an internal soft cannula tear that lets insulin leak inside the Pod instead of being delivered. 1,240,115 units are affected.

    Product
    Omnipod 5 Pods. Model/Catalog number: PT-001662 ASM 5PK Pod STRL OPS G6G7
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V256000·2026-04-22

    Toyota RAV4 front seat brackets may be welded improperly

    Toyota is recalling certain 2025 RAV4 vehicles because the front seat brackets for the seat rails may be welded improperly, which can prevent the seat from restraining an occupant in a crash.

    Product
    TOYOTA — TOYOTA RAV4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1803-2026·2026-04-22

    B. Braun 4.8 mm hemodialysis bloodlines may accumulate arterial air bubbles

    B. Braun is recalling hemodialysis bloodlines with a 4.8 mm pump segment because small air bubbles can accumulate in the arterial line under negative pressure. 4,884 units are affected.

    Product
    B Braun Hemodialysis Bloodlines, LOW VOL, NO CHAMBER 4.8MM PUMP SEGMENT. Model Number: B3-4630M4705.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1801-2026·2026-04-22

    B. Braun StreamLine long bloodlines may accumulate arterial air bubbles

    B. Braun is recalling StreamLine Bloodline Long Version sets because small air bubbles can accumulate in the arterial line under negative pressure. 328,640 units are affected.

    Product
    B. Barun Hemodialysis Bloodlines, StreamLine Bloodline Long Version, FMC. Model Number: SL-2000M2095L.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1802-2026·2026-04-22

    B. Braun hemodialysis bloodlines may accumulate air bubbles in the arterial line

    B. Braun is recalling one model of hemodialysis bloodline because small air bubbles can accumulate in the arterial line when blood gases adhere to the tubing under negative pressure.

    Product
    B. Braun Hemodialysis Bloodlines, LOW VOL, NO CHAMBER 2.6MM PUMP SEGMENT. Model Number: B3-3632M3705.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1798-2026·2026-04-22

    B. Braun StreamLine Dialog DR bloodlines may accumulate arterial air bubbles

    B. Braun is recalling StreamLine Bloodline Sets for Dialog DR because small air bubbles can accumulate in the arterial line under negative pressure. 3,158,104 units are affected.

    Product
    B. Braun Hemodialysis Bloodlines, STREAMLINE BLOODLINE SET FOR DIALOG DR. Model Number: SL-2010M2096A.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1800-2026·2026-04-22

    B. Braun StreamLine Fresenius bloodlines may accumulate arterial air bubbles

    B. Braun is recalling StreamLine Fresenius bloodlines supplied for DaVita because small air bubbles can accumulate in the arterial line under negative pressure. 1,174,271 units are affected.

    Product
    B. Braun Hemodialysis Bloodlines, STREAMLINE FRESENIUS FOR DAVITA. Model Number: SL-2000M2095DA.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0455-2026·2026-04-22

    SLMD benzoyl peroxide acne lotion recalled over benzene contamination

    SLMD Benzoyl Peroxide Acne Lotion, 2.5% benzoyl peroxide, is being recalled because of chemical contamination from the presence of benzene. 2,500 bottles are affected.

    Product
    SLMD Benzoyl Peroxide Acne Lotion, Benzoyl Peroxide 2.5%, a) 0.7 fl. oz - 21 mL and b) 1.5 fl. oz. - 44mL bottles, SANDRA LEE MD., Distributed by Skin PS Brands, Culver City, CA 90232.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1806-2026·2026-04-22

    Yeastone Broth recalled because it may report incorrect susceptibility results

    Yeastone Broth is being recalled because the product may report incorrect antifungal susceptibility results during quality control, which could delay treatment or force a change of agent.

    Product
    Yeastone Broth, 11ML, 10/BOX YY3462
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1818-2026·2026-04-22

    Cytal Wound Matrix 10x15 cm recalled over out-of-specification endotoxin results

    Cytal Wound Matrix 2-Layer 10x15 cm dressings are being recalled because of an increased rate of out-of-specification endotoxin results. 452 units are affected.

    Product
    Cytal Wound Matrix 2-Layer 10x15 cm. Product ID: WSM1015.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0483-2026·2026-04-22

    IMS epinephrine injection vials recalled over lack of sterility assurance

    International Medication Systems is recalling one lot of Epinephrine Injection, USP, 1 mg/10 mL, citing lack of assurance of sterility. 81,520 units are affected.

    Product
    EPINEPHRINE — EPINEPHRINE (EPINEPHRINE)
    Category
    Drug
    Distribution
    Distributed nationwide